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90539-80-3

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90539-80-3 Usage

Benzoylated derivative

3-cyanoindole 1-benzoyl-3-cyanoindole is derived from 3-cyanoindole by attaching a benzoyl group, making it a modified version of the original compound.

Versatile building block

Organic synthesis The compound serves as a useful intermediate in organic synthesis, allowing for the creation of various complex organic molecules.

Potential applications

Pharmaceutical and agrochemical industries Due to its diverse pharmacological activities, 1-benzoyl-3-cyanoindole can be used in the development of new drugs and agrochemicals.

Pharmacological activities

Anti-inflammatory, anti-cancer, and antimicrobial properties The compound exhibits a range of biological activities, making it a promising candidate for therapeutic and protective applications.

Fluorescent probe

Protein kinase C activity detection 1-benzoyl-3-cyanoindole has been studied for its potential use as a fluorescent probe in biochemical research, specifically for monitoring protein kinase C activity.

Synthesis of complex organic molecules

Novel drug candidates and agrochemicals The compound's ability to serve as a building block in organic synthesis contributes to the development of new and potentially innovative pharmaceutical and agrochemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 90539-80-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,5,3 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 90539-80:
(7*9)+(6*0)+(5*5)+(4*3)+(3*9)+(2*8)+(1*0)=143
143 % 10 = 3
So 90539-80-3 is a valid CAS Registry Number.

90539-80-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzoylindole-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 1H-Indole-3-carbonitrile,1-benzoyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:90539-80-3 SDS

90539-80-3Relevant articles and documents

On attempted Diels-Alder reaction of 1-ethoxycarbonylindole-3-carboxaldehyde N,N-dimethylhydrazone

Biswas,Nath,Mukherjee,Patra,Chakrabarty

, p. 117 - 118 (1992)

The reaction of 1-ethoxycarbonylindole-3-carboxaldehyde N,N-dimethylhydrazine with five dienophiles has been studied, and the first use of this new azadiene in a Diels-Alder reaction with N-methylmaleimide has been achieved leading to a new synthesis of a

Manganese(III) acetate initiated oxidative free radical reaction between benzoylindoles and dimethyl malonate

Wang, Sheow-Fong,Chuang, Che-Ping

, p. 347 - 359 (2007/10/03)

A free radical reaction between benzoylindoles and dimethyl malonate initiated by manganese(III) acetate is described. This free radical reaction provides a new method for the synthesis of indolo[1,2-b]isoquinolines and benzo[b]carbazoles. With meta subst

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